Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS

K-Number: K911180 · 1991-03-29

ApplicantNorthgate Technologies, Inc.
Decision Date1991-03-29
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K911180. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS?

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911180.

When did CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS receive FDA 510(k) clearance?

CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS received FDA 510(k) clearance on 1991-03-29, under 510(k) number K911180.

Who is the listed applicant for CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS?

The FDA 510(k) record lists Northgate Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS?

The FDA product code for CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS is HTD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Northgate Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K202813URO-TOUCH 9 French ProbeK202944NEBULAE SRS Laparoscopic Surgical Smoke Removal SystemK130368AUTOLITH TOUCH; URO TOUCHK120151NEBULAE IK041560FLO-ASSISTANTK033614MISTIC HUMIDIFICATION SYSTEM 850-00/01/02, 2215

View all 55 devices →

Related Devices (Code: HTD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK895212TIK EXTRAKTORInstruments of Sweden, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑